chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69375919	69375920	C	CATT	20	GENIC	homozygous	51485159
10	69383928	69383929	G	-	2	GENIC	homozygous	52383756
10	69383930	69383931	T	TGCTTG	2	GENIC	homozygous	52383758
10	69383935	69383936	G	GCA	2	GENIC	homozygous	52383760
10	69383938	69383939	T	C	2	GENIC	homozygous	52383762
10	69397948	69397949	G	GTC	5	GENIC	heterozygous	52441302
10	69397955	69397957	TC	--	5	GENIC	heterozygous	52461201
10	69407233	69407234	G	GTGCA	9	GENIC	homozygous	51485228
10	69408344	69408345	C	CA	20	GENIC	homozygous	51485230
10	69408354	69408355	G	-	22	GENIC	homozygous	51485231
10	69411336	69411337	G	-	19	GENIC	homozygous	51687143
10	69425096	69425097	T	TC	11	GENIC	homozygous	51485257
10	69425269	69425270	C	-	9	GENIC	heterozygous	51687149